A case of progressive subcortical gliosis presenting clinically as Steele-Richardson-Olszewski syndrome.
AUTOR(ES)
Will, R G
RESUMO
A patient presenting with the characteristic clinical features of Steele-Richardson-Olszewski syndrome is described, in whom neuropathological examination revealed atypical features, including extensive cortical and subcortical gliosis. The clinical and pathological features are discussed with particular reference to Creutzfeldt-Jacob disease and it is proposed that the case should be classified as progressive subcortical gliosis.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1033033Documentos Relacionados
- Cognitive deficits in the Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy).
- Focal paroxysmal kinesigenic choreoathetosis preceding the development of Steele-Richardson-Olszewski syndrome.
- Natural history of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) and clinical predictors of survival: a clinicopathological study.
- Differential diagnosis of Parkinson's disease, multiple system atrophy, and Steele-Richardson-Olszewski syndrome: discriminant analysis of striatal 18F-dopa PET data.
- A case of progressive subcortical gliosis associated with deposition of abnormal prion protein (PrP)